A genomic window into the virulence of Histophilus somni

Trends in Microbiology

Volumn 18, Issue 2, 2010, Pages 90-99

  Sandal, Indra ^a   Inzana, Thomas J ^a  

^a CENTER FOR MOLECULAR MEDICINE AND INFECTIOUS DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADHESIN; EXOPOLYSACCHARIDE; FERRIC UPTAKE REGULATOR; GENE PRODUCT; HEMAGGLUTININ; HEME; IMMUNOGLOBULIN BINDING FACTOR; LIPOOLIGOSACCHARIDE; OUTER MEMBRANE PROTEIN; PHOSPHORYLCHOLINE; POLYMER; PROTEIN TONB; TRANSFERRIN BINDING PROTEIN; VIRULENCE FACTOR;

BACTERIAL GENETICS; BACTERIAL STRAIN; BACTERIAL VIRULENCE; BACTERIUM ISOLATION; BIOFILM; GENE SEQUENCE; GENETIC SIMILARITY; HAEMOPHILUS INFLUENZAE; HISTOPHILUS SOMNI; NONHUMAN; NUCLEOTIDE SEQUENCE; PASTEURELLACEAE; PHENOTYPE; PREPUCE; PRIORITY JOURNAL; REVIEW; SEQUENCE HOMOLOGY; SITE DIRECTED MUTAGENESIS; SPECIES DIFFERENCE; TRANSPOSON; VIRUS CELL INTERACTION;

ANIMALS; CATTLE; CATTLE DISEASES; GENOME, BACTERIAL; GENOMICS; PASTEURELLACEAE; PASTEURELLACEAE INFECTIONS; SHEEP; SHEEP DISEASES; VIRULENCE; VIRULENCE FACTORS;

BACTERIA (MICROORGANISMS); BOS; BOVINAE; HAEMOPHILUS INFLUENZAE; HISTOPHILUS SOMNI; OVIS ARIES; PASTEURELLACEAE;

EID: 75349091218     PISSN: 0966842X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tim.2009.11.006     Document Type: Review

References (102)

1. Stephens L.R., et al. Morphological, biochemical, antigenic, and cytochemical relationships among Haemophilus somnus, Haemophilus agni, Haemophilus haemoglobinophilus, Histophilus ovis, and Actinobacillus seminis. J. Clin. Microbiol. 17 (1983) 728-737
2. Angen O., et al. Proposal of Histophilus somni gen. nov., sp. nov. for the three species incertae sedis 'Haemophilus somnus', 'Haemophilus agni' and 'Histophilus ovis'. Int. J. Syst. Evol. Microbiol. 53 (2003) 1449-1456
3. Olsen I., Moller K., et al. Family I. Pasteurellaceae Pohl 1981b, 382VP. In: Garrity G.M., et al. (Ed). Bergey's Manual of Systematic Bacteriology: Vol. 2, The Proteobacteria, Part B, The Gammaproteobacteria. 2nd edn (2005), Springer 851-856
4. Gagea M.I., et al. Diseases and pathogens associated with mortality in Ontario beef feedlots. J. Vet. Diagn. Invest. 18 (2006) 18-28
5. Kennedy P.C., et al. Infectious meningo-encephalitis in cattle, caused by a haemophilus-like organism. Am. J. Vet. Res. 21 (1960) 403-409
6. Humphrey J.D., and Stephens L.R. Haemophilus somnus: a review. Vet. Bull. 53 (1983) 987-1004
7. Miller R.B., et al. Haemophilus somnus infection of the reproductive tract of cattle: a review. J. Am. Vet. Med. Assoc. 182 (1983) 1390-1392
8. Corbeil L.B., et al. Serum susceptibility of Haemophilus somnus from bovine clinical cases and carriers. J. Clin. Microbiol. 22 (1985) 192-198
9. Howard M.D., et al. Inhibition of bovine macrophage and polymorphonuclear leukocyte superoxide anion production by Haemophilus somnus. Microb. Pathog. 37 (2004) 263-271
10. Howard M.D., et al. Antigenic diversity of Haemophilus somnus lipooligosaccharide: phase-variable accessibility of the phosphorylcholine epitope. J. Clin. Microbiol. 38 (2000) 4412-4419
11. Inzana T.J., et al. Incorporation of N-acetylneuraminic acid into Haemophilus somnus lipooligosaccharide (LOS): enhancement of resistance to serum and reduction of LOS antibody binding. Infect. Immun. 70 (2002) 4870-4879
12. McQuiston J.H., et al. Characterization of a DNA region containing 5′-CAAT-3′ DNA sequences involved in lipooligosaccharide biosynthesis in Haemophilus somnus. Microb. Pathogen. 28 (2000) 301-312
13. Sandal I., et al. Characterization and comparison of biofilm development by pathogenic and commensal isolates of Histophilus somni. J. Bacteriol. 189 (2007) 8179-8185
14. Wu Y., et al. Molecular cloning and mutagenesis of a DNA locus involved in lipooligosaccharide biosynthesis in Haemophilus somnus. Infect. Immun. 68 (2000) 310-319
15. Cole S.P., et al. Two linked genes for outer membrane proteins are absent in four non-disease strains of Haemophilus somnus. Mol. Microbiol. 6 (1992) 1895-1902
16. Widders P.R., et al. Immunoglobulin-binding activity among pathogenic and carrier isolates of Haemophilus somnus. Infect. Immun. 57 (1989) 639-642
17. Challacombe J.F., et al. Complete genome sequence of Haemophilus somnus (Histophilus somni) strain 129Pt and comparison to Haemophilus ducreyi 35000HP and Haemophilus influenzae Rd. J. Bacteriol. 189 (2007) 1890-1898
18. Challacombe, J.F. and Inzana, T.J. (2008) Chapter 3: Comparative genomics of Pasteurellaceae. In Pasteurellaceae: Biology, Genomics and Molecular Aspects (Kuhnert, P. and Christensen, H., eds), pp. 53-77, Caister Academic Press
19. Tagawa Y., et al. Genetic and functional analysis of Haemophilus somnus high molecular weight-immunoglobulin binding proteins. Microb. Pathog. 39 (2005) 159-170
20. Ward C.K., et al. Haemophilus ducreyi secretes a filamentous hemagglutinin-like protein. J. Bacteriol. 180 (1998) 6013-6022
21. Kobayashi I. Behavior of restriction-modification systems as selfish mobile elements and their impact on genome evolution. Nucl. Acids Res. 29 (2001) 3742-3756
22. Cox A.D., et al. Structural analysis of the phase-variable lipooligosaccharide from Haemophilus somnus strain 738. Eur. J. Biochem. 253 (1998) 507-516
23. St Michael F., et al. Structural analysis of the oligosaccharide of Histophilus somni (Haemophilus somnus) strain 2336 and identification of several lipooligosaccharide biosynthesis gene homologues. Carbohydr. Res. 340 (2005) 665-672
24. Preston A., et al. The lipopolysaccharides of pathogenic gram-negative bacteria. Crit. Rev. Microbiol. 22 (1996) 139-180
25. Elswaifi S.F., et al. Molecular characterization of phosphorylcholine expression on the lipooligosaccharide of Histophilus somni. Microb. Pathog. 47 (2009) 223-230
26. Inzana T.J., et al. Phase variation and conservation of lipooligosaccharide epitopes in Haemophilus somnus. Infect. Immun. 65 (1997) 4675-4681
27. Kanda T., et al. Isolation and culture of bovine endothelial cells of endoneurial origin. J. Neurosci. Res. 49 (1997) 769-777
28. Moran A.P., et al. Molecular mimicry of host structures by bacterial lipopolysaccharides and its contribution to disease. FEMS Immunol. Med. Microbiol. 16 (1996) 105-115
29. Schweda E.K., et al. Expression and structural diversity of the lipopolysaccharide of Haemophilus influenzae: implication in virulence. Int. J. Med. Microbiol. 297 (2007) 297-306
30. Johnston J.W., et al. Regulation of sialic acid transport and catabolism in Haemophilus influenzae. Mol. Microbiol. 66 (2007) 26-39
31. Swords W.E., et al. Non-typeable Haemophilus influenzae adhere to and invade human bronchial epithelial cells via an interaction of lipooligosaccharide with the PAF receptor. Mol. Microbiol. 37 (2000) 13-27
32. Weiser J.N., et al. Phosphorylcholine on the lipopolysaccharide of Haemophilus influenzae contributes to persistence in the respiratory tract and sensitivity to serum killing mediated by C-reactive protein. J. Exp. Med. 187 (1998) 631-640
33. Kuckleburg C.J., et al. Expression of phosphorylcholine by Histophilus somni induces bovine platelet aggregation. Infect. Immun. 75 (2007) 1045-1049
34. Weiser J.N., et al. Decoration of lipopolysaccharide with phosphorylcholine: a phase-variable characteristic of Haemophilus influenzae. Infect. Immun. 65 (1997) 943-950
35. Corbeil L.B. Histophilus somni host-parasite relationships. Anim. Health Res. Rev. 8 (2007) 151-160
36. Geertsema R.S., et al. Bovine plasma proteins increase virulence of Haemophilus somnus in mice. Microb. Pathog. 42 (2007) 22-28
37. Corbeil L.B., et al. Haemophilus somnus immunoglobulin binding proteins and surface fibrils. Infect. Immun. 65 (1997) 4250-4257
38. Corbeil L.B., et al. Antigenic specificity of convalescent serum from cattle with Haemophilus somnus-induced experimental abortion. Infect. Immun. 55 (1987) 1381-1386
39. Yarnall M., et al. Isolation and characterization of Fc receptors from Haemophilus somnus. Scand. J. Immunol. 28 (1988) 129-137
40. Bastida-Corcuera F.D., et al. Binding of bovine IgG2a and IgG2b allotypes to protein A, protein G, and Haemophilus somnus IgBPs. Vet. Immunol. Immunopathol. 71 (1999) 143-149
41. Yarnall M., and Corbeil L.B. Antibody response to Haemophilus somnus Fc receptor. J. Clin. Microbiol. 27 (1989) 111-117
42. Jacob-Dubuisson F., et al. Two-partner secretion in Gram-negative bacteria: a thrifty, specific pathway for large virulence proteins. Mol. Microbiol. 40 (2001) 306-313
43. Blom J., et al. Morphology of cells and hemagglutinogens of Bordetella species: resolution of substructural units in fimbriae of Bordetella pertussis. Infect. Immun. 42 (1983) 308-317
44. May B.J., et al. Complete genomic sequence of Pasteurella multocida Pm70. Proc. Natl. Acad. Sci. U. S. A. 98 (2001) 3460-3465
45. Shao F., et al. A Yersinia effector and a Pseudomonas avirulence protein define a family of cysteine proteases functioning in bacterial pathogenesis. Cell 109 (2002) 575-588
46. Geertsema R.S., et al. Protection of mice against H. somni septicemia by vaccination with recombinant immunoglobulin binding protein subunits. Vaccine 26 (2008) 4506-4512
47. Worby C.A., et al. The fic domain: regulation of cell signaling by adenylylation. Mol. Cell 34 (2009) 93-103
48. Hoshinoo K., et al. Virulence attributes of Histophilus somni with a deletion mutation in the ibpA gene. Microb. Pathog. 46 (2009) 273-282
49. Jansen E.D. The Haemophilus somnus disease complex: a review. Can. Vet. J. 30 (1989) 816-822
50. Sylte M.J., et al. Haemophilus somnus induces apoptosis in bovine endothelial cells in vitro. Infect. Immun. 69 (2001) 1650-1660
51. Behling-Kelly E., et al. Haemophilus somnus activation of brain endothelial cells: potential role for local cytokine production and thrombosis in central nervous system (CNS) infection. Thromb. Haemost. 98 (2007) 823-830
52. Kuckleburg C.J., et al. Platelet activation by Histophilus somni and its lipooligosaccharide induces endothelial cell proinflammatory responses and platelet internalization. Shock 29 (2008) 189-196
53. Kuckleburg C.J., et al. Bovine platelets activated by Haemophilus somnus and its LOS induce apoptosis in bovine endothelial cells. Microb. Pathog. 38 (2005) 23-32
54. Ruby K.W., et al. Histamine production by Haemophilus somnus. Comp. Immunol. Microbiol. Infect. Dis. 25 (2002) 13-20
55. Behling-Kelly E., and Czuprynski C.J. Endothelial cells as active participants in veterinary infections and inflammatory disorders. Anim. Health Res. Rev. 8 (2007) 47-58
56. Czuprynski C.J., et al. Complexities of the pathogenesis of Mannheimia haemolytica and Haemophilus somnus infections: challenges and potential opportunities for prevention? Anim. Health Res. Rev. 5 (2004) 277-282
57. Siddaramppa S., and Inzana T.J. Haemophilus somnus virulence factors and resistance to host immunity. Anim. Health Res. Rev. 5 (2004) 79-93
58. Gomis S.M. Intracellular survival of Haemophilus somnus in bovine blood monocytes and alveolar macrophages. Microb. Pathog. 25 (1998) 227-235
59. Lederer J.A., et al. 'Haemophilus somnus', a facultative intracellular pathogen of bovine mononuclear phagocytes. Infect. Immun. 55 (1987) 381-387
60. Yang Y.F., et al. Apoptosis: a possible tactic of Haemophilus somnus for evasion of killing by bovine neutrophils? Microb. Pathog. 24 (1998) 351-359
61. Donlan R.M., and Costerton J.W. Biofilms: survival mechanisms of clinically relevant microorganisms. Clin. Microbiol. Rev. 15 (2002) 167-193
62. Olson M.E., et al. Biofilm bacteria: formation and comparative susceptibility to antibiotics. Can. J. Vet. Res. 66 (2002) 86-92
63. Kaplan J.B., and Mulks M.H. Biofilm formation is prevalent among field isolates of Actinobacillus pleuropneumoniae. Vet. Microbiol. 108 (2005) 89-94
64. Jin H., et al. Biofilm formation by field isolates and reference strains of Haemophilus parasuis. Vet. Microbiol. 118 (2006) 117-123
65. Kaplan J.B., et al. Biofilm growth and detachment of Actinobacillus actinomycetemcomitans. J. Bacteriol. 185 (2003) 1399-1404
66. Murphy T.F., and Kirkham C. Biofilm formation by nontypable Haemophilus influenzae: strain variability, outer membrane antigen expression and role of pili. BMC Microbiol. 2 (2002) 7
67. Galli J., et al. Biofilm formation by Haemophilus influenzae isolated from adeno-tonsil tissue samples, and its role in recurrent adenotonsillitis. Acta Otolaryngol. 27 (2007) 134-138
68. Hall-Stoodley L., et al. Direct detection of bacterial biofilms on the middle ear mucosa of children with chronic otitis media. J. Am. Med. Assoc. 296 (2006) 202-211
69. Sanderson A.R., et al. Bacterial biofilms on the sinus mucosa of human subjects with chronic rhinosinusitis. Laryngoscope 116 (2006) 1121-1126
70. Sandal I., et al. Histophilus somni biofilm formation in cardiopulmonary tissue of the bovine host following respiratory challenge. Microbes Infect. 11 (2009) 254-263
71. Watnick P., and Kolter R. Biofilm, city of microbes. J. Bacteriol. 182 (2000) 2675-2679
72. Flemming H.C., et al. The EPS matrix: the 'house of biofilm cells'. J Bacteriol 189 (2007) 7945-7947
73. Jackson K.D., et al. Identification of psl, a locus encoding a potential exopolysaccharide that is essential for Pseudomonas aeruginosa PAO1 biofilm formation. J. Bacteriol. 186 (2004) 4466-4475
74. Ryder C., et al. Role of polysaccharides in Pseudomonas aeruginosa biofilm development. Curr. Opin. Microbiol. 10 (2007) 644-648
75. Sanders J.D., et al. Genetic manipulation of immunoglobulin binding proteins of Haemophilus somnus. Microb. Pathog. 34 (2003) 131-139
76. Dixon L.G., et al. An analysis of the complete nucleotide sequence of the Haemophilus ducreyi broad-host-range plasmid pLS88. Plasmid 32 (1994) 228-232
77. Sanders J.D., et al. Transformation of a virulence associated gene of Haemophilus somnus into a strain lacking the gene. FEMS Microbiol. Lett. 154 (1997) 251-258
78. Briggs R.E., and Tatum F.M. Generation and molecular characterization of new temperature-sensitive plasmids intended for genetic engineering of Pasteurellaceae. Appl. Environ. Microbiol. 71 (2005) 7187-7195
79. Sandal I., et al. Construction of a high-efficiency shuttle vector for Histophilus somni. J. Microbiol. Methods 74 (2008) 106-109
80. Kajava A.V., et al. Beta-helix model for the filamentous haemagglutinin adhesin of Bordetella pertussis and related bacterial secretory proteins. Mol. Microbiol. 42 (2001) 279-292
81. Chen I., and Dubnau D. DNA uptake during bacterial transformation. Nat. Rev. Microbiol. 2 (2004) 241-249
82. Redfield R.J., et al. Evolution of competence and DNA uptake specificity in the Pasteurellaceae. BMC Evol. Biol. 6 (2006) 82
83. Bakkali M., et al. Evolutionary stability of DNA uptake signal sequences in the Pasteurellaceae. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 4513-4518
84. St Michael F., et al. Structural analysis of the lipooligosaccharide from the commensal Haemophilus somnus genome strain 129Pt. Carbohydr. Res. 339 (2004) 529-535
85. Yarnall M., et al. Characterization of two Haemophilus somnus Fc receptors. J. Gen. Microbiol. 134 (1988) 1993-1999
86. Widders P.R., et al. Non-immune immunoglobulin binding by 'Haemophilus somnus'. J. Med. Microbiol. 26 (1988) 307-311
87. Corbeil L.B., et al. Bovine IgG2a antibodies to Haemophilus somnus and allotype expression. Can. J. Vet. Res. 61 (1997) 207-213
88. Gogolewski R.P., et al. Protective ability and specificity of convalescent serum from calves with Haemophilus somnus pneumonia. Infect. Immun. 55 (1987) 1403-1411
89. Gogolewski R.P., et al. Protective ability of antibodies against 78- and 40-kilodalton outer membrane antigens of Haemophilus somnus. Infect. Immun. 56 (1988) 2307-2316
90. Corbeil L.B., et al. Characterization of immunodominant surface antigens of Haemophilus somnus. Infect. Immun. 59 (1991) 4295-4301
91. Tagawa Y., et al. Antigenic analysis of the major outer membrane protein of Haemophilus somnus with monoclonal antibodies. Infect. Immun. 61 (1993) 2257-2259
92. Tagawa Y., et al. Purification and partial characterization of the major outer membrane protein of Haemophilus somnus. Infect. Immun. 61 (1993) 91-96
93. Khan M.S., et al. Molecular characterization of the major outer membrane protein of Haemophilus somnus. Vet. Microbiol. 107 (2005) 179-192
94. Tagawa Y., et al. Characterization of a heat-modifiable outer membrane protein of Haemophilus somnus. Infect. Immun. 61 (1993) 1750-1755
95. Tagawa Y., et al. Characterization of an immunoreactive 17.5-kilodalton outer membrane protein of Haemophilus somnus by using a monoclonal antibody. Infect. Immun. 61 (1993) 4153-4157
96. Won J., and Griffith R.W. Cloning and sequencing of the gene encoding a 31-kilodalton antigen of Haemophilus somnus. Infect. Immun. 61 (1993) 2813-2821
97. Corbeil L.B., et al. Cloning and expression of genes encoding Haemophilus somnus antigens. Infect. Immun. 56 (1988) 2736-2742
98. Kania S.A., et al. Characterization of a 78-kilodalton outer membrane protein of Haemophilus somnus. Infect. Immun. 58 (1990) 237-244
99. Theisen M., et al. Molecular cloning, nucleotide sequence, and characterization of a 40,000-molecular-weight lipoprotein of Haemophilus somnus. Infect. Immun. 60 (1992) 826-831
100. Theisen M., et al. Molecular cloning, nucleotide sequence, and characterization of lppB, encoding an antigenic 40-kilodalton lipoprotein of Haemophilus somnus. Infect. Immun. 61 (1993) 1793-1798
101. Ogunnariwo J.A., et al. Response of Haemophilus somnus to iron limitation: expression and identification of a bovine-specific transferrin receptor. Microb. Pathog. 9 (1990) 397-406
102. Ekins A., et al. Haemophilus somnus possesses two systems for acquisition of transferrin-bound iron. J. Bacteriol. 186 (2004) 4407-4411